Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs786201059
TP53
0.701 0.360 17 7673764 stop gained C/A;G;T snv 19
rs121912660
TP53
0.683 0.240 17 7673781 missense variant C/A;G;T snv 18
rs760043106
TP53
0.645 0.440 17 7674947 missense variant A/C;G;T snv 18
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv 18
rs1057519747
TP53
0.716 0.280 17 7675094 missense variant A/C;G;T snv 17
rs1057519946
PPP2R1A
0.732 0.280 19 52212729 missense variant C/G;T snv 17
rs121913400
CTNNB1
0.683 0.360 3 41224610 missense variant C/A;G;T snv 17
rs28933406
LRRC56 ; HRAS
0.667 0.480 11 533875 missense variant G/C;T snv 17
rs587780073
TP53
0.708 0.400 17 7674262 missense variant T/C;G snv 17
rs864622237
TP53
0.716 0.320 17 7674263 missense variant A/C;G;T snv 17
rs866775781
TP53
0.716 0.440 17 7675216 splice acceptor variant C/A;G snv 17
rs1057519985
TP53
0.724 0.360 17 7673763 missense variant T/A;C;G snv 16
rs1057519996
TP53
0.701 0.360 17 7675217 splice acceptor variant T/A;C;G snv 16
rs587782329
TP53
0.677 0.280 17 7674217 missense variant C/A;G;T snv 16
rs942158624
TP53
0.724 0.320 17 7674948 missense variant T/A snv 16
rs967461896
TP53
0.724 0.240 17 7675086 missense variant A/C;G;T snv 16
rs985033810
TP53
0.724 0.280 17 7674232 missense variant C/A;G;T snv 16
rs1057519895
FBXW7
0.724 0.240 4 152328232 missense variant C/A;G;T snv 15
rs1057519989
TP53
0.732 0.240 17 7674233 missense variant C/A;G;T snv 15
rs121912655
TP53
0.724 0.400 17 7674238 missense variant C/A;G;T snv 15
rs121913495
GNAS
0.672 0.400 20 58909366 missense variant G/A;T snv 15
rs397517201
PIK3CA
0.732 0.240 3 179218307 missense variant A/C;G;T snv 15
rs121913403
CTNNB1
0.683 0.240 3 41224622 missense variant C/A;G;T snv 14
rs28931588
CTNNB1
0.701 0.200 3 41224606 missense variant G/A;C;T snv 14
rs377767347
SMAD4
0.742 0.520 18 51065549 missense variant G/A;C;T snv 14